Microwave-promoted synthesis of ?-hydroxyesters by the Reformatsky reaction in the absence of solvent
A microwave-promoted Reformatsky reaction of aldehydes and ketones with ethyl bromoacetate, in the absence of solvent, using activated zinc metal and solid NH4Cl afforded the corresponding ?-hydroxyesters in good to excellent yields.
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Veröffentlicht in: | Journal of chemical research 2003-06, Vol.2003 (6), p.374-376 |
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container_issue | 6 |
container_start_page | 374 |
container_title | Journal of chemical research |
container_volume | 2003 |
creator | Gholap, Atul R Chavan, Abhijit P |
description | A microwave-promoted Reformatsky reaction of aldehydes and ketones with ethyl bromoacetate, in the absence of solvent, using activated zinc metal and solid NH4Cl afforded the corresponding ?-hydroxyesters in good to excellent yields. |
doi_str_mv | 10.3184/030823403103174209 |
format | Article |
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source | SAGE Journals |
subjects | Activated |
title | Microwave-promoted synthesis of ?-hydroxyesters by the Reformatsky reaction in the absence of solvent |
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